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Clinical Trials/NCT07395999
NCT07395999
Completed
Not Applicable

Effectiveness of Pain Management Interventions in Patients With Chronic Cancer Pain in a Tertiary Care Hospital: A Retrospective Audit

Aga Khan University1 site in 1 country134 target enrollmentStarted: November 14, 2025Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
134
Locations
1
Primary Endpoint
Patient reported NRS score

Overview

Brief Summary

The goal of this observational study is to observe the effectiveness of pain management strategies in patients with chronic cancer pain presenting to pain management clinic at Aga Khan University.

The main question[s] it aims to answer are:

  • What is the overall effectiveness of pain management techniques in patients with chronic cancer pain?
  • What is the character and severity of pain?
  • What is the frequency of pain intervention procedures?

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All adult patients
  • Patients with chronic cancer pain

Exclusion Criteria

  • Patients lost to follow-up after the initial visit.

Arms & Interventions

Patients with Chronic cancer pain

Patients with chronic cancer pain receiving pain management intervention

Intervention: Pharmacological and pain Intervention procedure (Other)

Outcomes

Primary Outcomes

Patient reported NRS score

Time Frame: Patient reported NRS score will be recorded at baseline, and subsequent visit (till maximum three months) in the pain management clinic.

Numeric Rating Score (NRS) is an 11-point scale with scores ranging from 0 (no pain) to 10 (worst imaginable pain), with higher scores indicating greater pain severity and therefore a worse outcome.

Secondary Outcomes

  • Character of chronic pain(At baseline and the follow-up visit ( till maximum three months) to the pain management clinic.)
  • Frequency of pain intervention procedure(At the end of three months.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ali Sarfraz Siddiqui

Associate Professor

Aga Khan University

Study Sites (1)

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